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人B、T淋巴细胞衰减因子(BTLA)微量上样酶联免疫吸附检测试剂盒

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ELK8669MS

规格：	价格：
48T	￥1960.00
96T	￥2800.00

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Overview

Product name:	Human BTLA(B- and T-lymphocyte attenuator) Microsample ELISA Kit
Reactivity:	Human
Alternative Names:	B and T lymphocyte associated protein; B and T lymphocyte attenuator; B and T lymphocyte associated; B- and T-lymphocyte attenuator; B- and T-lymphocyte-associated protein; BTLA; BTLA_HUMAN; BTLA1; CD272; CD272 antigen; FLJ16065; MGC129743
Assay Type:	Sandwich
Sensitivity:	0.22 ng/mL
Standard:	30 ng/mL
Detection Range:	0.47-30 ng/mL
Sample Type:	Serum, plasma, urine, tissue homogenates, cell culture supernates and other biological fluids
Assay Length:	3.5h
Research Area:	Cardiac function; Cancer
Uniprot ID:	BTLA
Test principle:	The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human BTLA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human BTLA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human BTLA, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human BTLA in the samples is then determined by comparing the OD of the samples to the standard curve.

标准曲线

Concentration (ng/mL)	OD	Corrected OD
30.00	2.607	2.517
15.00	1.499	1.409
7.50	1.170	1.080
3.75	0.730	0.640
1.88	0.547	0.457
0.94	0.313	0.223
0.47	0.230	0.140
0.00	0.090	0.000

精密度

Intra-assay Precision (Precision within an assay)：CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays)：CV%<10%

Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.

回收率

Matrices listed below were spiked with certain level of recombinant BTLA and the recovery rates were calculated by comparing the measured value to the expected amount of BTLA in samples.

Matrix	Recovery range	Average
serum(n=5)	86-116%	101%
EDTA plasma(n=5)	87-124%	106%
Heparin plasma(n=5)	82-120%	101%

线性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of BTLA and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.